Departamento de Biología, Facultad de Química, Universidad Nacional Autónoma de México, Ciudad Universitaria, Coyoacán DF, México City 04510, Mexico.
Eur J Med Chem. 2013 Feb;60:350-9. doi: 10.1016/j.ejmech.2012.12.021. Epub 2012 Dec 17.
As a part of our research in the chemistry of chalcones we have prepared four pyrimidine monoadducts of bis-chalcones through the reaction with 6-amino-1,3-dimethyl uracil. These compounds displayed cytotoxicity with a massive vacuolation in different human cell lines in vitro. Compound 6 was the most cytotoxic inducer of vacuoles, this compound induced G1 phase cell cycle arrest, and their cytotoxicity went without morphological and biochemical evidence of apoptotic cell death in HeLa cells. In addition, our results showed that this vacuole formation does not require de novo protein synthesis and the content vacuolar is acidic. Compound 6 induce necrotic cell death with excessive vacuolation, similar to a process of autophagy. Spautin-1 an inhibitor of autophagy, decreased the transformation of microtubule-associated protein 1 light chain 3 (LC3B-I) to LC3B-II and the vacuolation induced by compound 6 in HeLa cells, both autophagy processes. These compounds could be of pivotal importance in the study of non-apoptotic cell death with vacuole formation and could be useful in research into new autophagy inhibitors agents.
作为我们查耳酮化学研究的一部分,我们通过与 6-氨基-1,3-二甲基尿嘧啶反应,制备了四个双查耳酮的嘧啶单加成物。这些化合物在体外对不同的人细胞系显示出细胞毒性,伴有大量空泡化。化合物 6 是诱导空泡化的最具细胞毒性的诱导剂,该化合物诱导 G1 期细胞周期停滞,并且在 HeLa 细胞中没有凋亡细胞死亡的形态和生化证据表明其具有细胞毒性。此外,我们的结果表明,这种空泡形成不需要新的蛋白质合成,并且空泡内容物呈酸性。化合物 6 诱导过度空泡化的坏死细胞死亡,类似于自噬过程。自噬抑制剂 Spautin-1 降低了微管相关蛋白 1 轻链 3(LC3B-I)向 LC3B-II 的转化,以及化合物 6 在 HeLa 细胞中诱导的空泡化,这两种自噬过程。这些化合物在研究具有空泡形成的非凋亡性细胞死亡方面可能具有重要意义,并且在研究新的自噬抑制剂方面可能有用。